Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_provenance.
- NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_assertion description "[These results suggest that CACNA1C may be associated with secondary hyperparathyroidism. In addition, the haplotype-based approach may be useful to screen for key molecules associated with complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_provenance.
- NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_assertion evidence source_evidence_literature NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_provenance.
- NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_assertion SIO_000772 20424473 NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_provenance.
- NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_assertion wasDerivedFrom gad-20130706 NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_provenance.
- NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_assertion wasGeneratedBy ECO_0000203 NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_provenance.
- gad-20130706 importedOn "2013-07-06" NP83619.RAeCWFULL3GujmkE2-mmMwJBi5ZPxeVw248o0r2sGnEzw130_provenance.